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Environment sensing and response mediated by ABC transporters

BACKGROUND: Transporter proteins are one of an organism’s primary interfaces with the environment. The expressed set of transporters mediates cellular metabolic capabilities and influences signal transduction pathways and regulatory networks. The functional annotation of most transporters is current...

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Autores principales: Giuliani, Sarah E, Frank, Ashley M, Corgliano, Danielle M, Seifert, Catherine, Hauser, Loren, Collart, Frank R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223731/
https://www.ncbi.nlm.nih.gov/pubmed/21810210
http://dx.doi.org/10.1186/1471-2164-12-S1-S8
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author Giuliani, Sarah E
Frank, Ashley M
Corgliano, Danielle M
Seifert, Catherine
Hauser, Loren
Collart, Frank R
author_facet Giuliani, Sarah E
Frank, Ashley M
Corgliano, Danielle M
Seifert, Catherine
Hauser, Loren
Collart, Frank R
author_sort Giuliani, Sarah E
collection PubMed
description BACKGROUND: Transporter proteins are one of an organism’s primary interfaces with the environment. The expressed set of transporters mediates cellular metabolic capabilities and influences signal transduction pathways and regulatory networks. The functional annotation of most transporters is currently limited to general classification into families. The development of capabilities to map ligands with specific transporters would improve our knowledge of the function of these proteins, improve the annotation of related genomes, and facilitate predictions for their role in cellular responses to environmental changes. RESULTS: To improve the utility of the functional annotation for ABC transporters, we expressed and purified the set of solute binding proteins from Rhodopseudomonas palustris and characterized their ligand-binding specificity. Our approach utilized ligand libraries consisting of environmental and cellular metabolic compounds, and fluorescence thermal shift based high throughput ligand binding screens. This process resulted in the identification of specific binding ligands for approximately 64% of the purified and screened proteins. The collection of binding ligands is representative of common functionalities associated with many bacterial organisms as well as specific capabilities linked to the ecological niche occupied by R. palustris. CONCLUSION: The functional screen identified specific ligands that bound to ABC transporter periplasmic binding subunits from R. palustris. These assignments provide unique insight for the metabolic capabilities of this organism and are consistent with the ecological niche of strain isolation. This functional insight can be used to improve the annotation of related organisms and provides a route to evaluate the evolution of this important and diverse group of transporter proteins.
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spelling pubmed-32237312011-11-26 Environment sensing and response mediated by ABC transporters Giuliani, Sarah E Frank, Ashley M Corgliano, Danielle M Seifert, Catherine Hauser, Loren Collart, Frank R BMC Genomics Research BACKGROUND: Transporter proteins are one of an organism’s primary interfaces with the environment. The expressed set of transporters mediates cellular metabolic capabilities and influences signal transduction pathways and regulatory networks. The functional annotation of most transporters is currently limited to general classification into families. The development of capabilities to map ligands with specific transporters would improve our knowledge of the function of these proteins, improve the annotation of related genomes, and facilitate predictions for their role in cellular responses to environmental changes. RESULTS: To improve the utility of the functional annotation for ABC transporters, we expressed and purified the set of solute binding proteins from Rhodopseudomonas palustris and characterized their ligand-binding specificity. Our approach utilized ligand libraries consisting of environmental and cellular metabolic compounds, and fluorescence thermal shift based high throughput ligand binding screens. This process resulted in the identification of specific binding ligands for approximately 64% of the purified and screened proteins. The collection of binding ligands is representative of common functionalities associated with many bacterial organisms as well as specific capabilities linked to the ecological niche occupied by R. palustris. CONCLUSION: The functional screen identified specific ligands that bound to ABC transporter periplasmic binding subunits from R. palustris. These assignments provide unique insight for the metabolic capabilities of this organism and are consistent with the ecological niche of strain isolation. This functional insight can be used to improve the annotation of related organisms and provides a route to evaluate the evolution of this important and diverse group of transporter proteins. BioMed Central 2011-06-15 /pmc/articles/PMC3223731/ /pubmed/21810210 http://dx.doi.org/10.1186/1471-2164-12-S1-S8 Text en Copyright ©2011 Giuliani et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Giuliani, Sarah E
Frank, Ashley M
Corgliano, Danielle M
Seifert, Catherine
Hauser, Loren
Collart, Frank R
Environment sensing and response mediated by ABC transporters
title Environment sensing and response mediated by ABC transporters
title_full Environment sensing and response mediated by ABC transporters
title_fullStr Environment sensing and response mediated by ABC transporters
title_full_unstemmed Environment sensing and response mediated by ABC transporters
title_short Environment sensing and response mediated by ABC transporters
title_sort environment sensing and response mediated by abc transporters
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223731/
https://www.ncbi.nlm.nih.gov/pubmed/21810210
http://dx.doi.org/10.1186/1471-2164-12-S1-S8
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